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HaploVar: Defining Local Haplotype Variants for Use in Trait Associationand Trait Prediction Analyses

A local haplotyping tool for use in trait association and trait prediction analyses pipelines. 'HaploVar' enables users take single nucleotide polymorphisms (SNPs) (in VCF format) and a linkage disequilibrium (LD) matrix, calculate local haplotypes and format the output to be compatible with a wide range of trait association and trait prediction tools. The local haplotypes are calculated from the LD matrix using a clustering algorithm called density-based spatial clustering of applications with noise ('DBSCAN') (Ester et al., 1996) <ISBN: 1577350049>.

Version:0.1.1
Depends:R (≥ 4.00)
Imports:dplyr,tidyr,tibble,magrittr,dbscan
Suggests:knitr,rmarkdown
Published:2025-07-21
DOI:10.32614/CRAN.package.HaploVar
Author:Tessa MacNishORCID iD [aut, cre], Hawlader Al-Mamun [ctb], Thomas Bergmann [ctb], Mitchell Bestry [ctb], Jacob Marsh [ctb], David Edwards [ctb]
Maintainer:Tessa MacNish <tessa.macnish at research.uwa.edu.au>
License:MIT + fileLICENSE
NeedsCompilation:no
CRAN checks:HaploVar results

Documentation:

Reference manual:HaploVar.html ,HaploVar.pdf
Vignettes:introduction (source,R code)

Downloads:

Package source: HaploVar_0.1.1.tar.gz
Windows binaries: r-devel:HaploVar_0.1.1.zip, r-release:HaploVar_0.1.1.zip, r-oldrel:HaploVar_0.1.1.zip
macOS binaries: r-release (arm64):HaploVar_0.1.1.tgz, r-oldrel (arm64):HaploVar_0.1.1.tgz, r-release (x86_64):HaploVar_0.1.1.tgz, r-oldrel (x86_64):HaploVar_0.1.1.tgz

Linking:

Please use the canonical formhttps://CRAN.R-project.org/package=HaploVarto link to this page.


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